The 5-HT1A receptor PET radioligand 11C-CUMI-101 has significant binding to α1-adrenoceptors in human cerebellum, limiting its use as a reference region

Abstract

Prazosin, a potent and selective a1-adrenoceptor antagonist, displaces 25% of 11C-CUMI-101 ([O-methyl-11C]2-(4-(4-(2-methoxyphenyl) piperazin-1-yl)butyl)-4-methyl-1,2,4-triazine-3,5(2H,4H)dione) binding in monkey cerebellum. We sought to estimate the percentage contamination of 11C-CUMI-101 binding to a1-adrenoceptors in human cerebellum under in vivo conditions. In vitro receptor-binding techniques were used to measure a1-adrenoceptor density and the affinity of CUMI-101 for these receptors in human, monkey, and rat cerebellum. Methods: Binding potential (maximum number of binding sites × affinity [(1/dissociation constant]) was determined using in vitro homogenate binding assays in human, monkey, and rat cerebellum. 3H-prazosin was used to determine the maximum number of binding sites, as well as the dissociation constant of 3H-prazosin and the inhibition constant of CUMI-101. Results: a1-adrenoceptor density and the affinity of CUMI-101 for these receptors were similar across species. Cerebellar binding potentials were 3.7 for humans, 2.3 for monkeys, and 3.4 for rats. Conclusion: Reasoning by analogy, 25% of 11C-CUMI-101 uptake in human cerebellum reflects binding to a1-adrenoceptors, suggesting that the cerebellum is of limited usefulness as a reference tissue for quantification in human studies.